- Trials with a EudraCT protocol (28)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28 result(s) found for: Nociceptive pain.
Displaying page 1 of 2.
EudraCT Number: 2009-016907-41 | Sponsor Protocol Number: fMRT-Nociception | Start Date*: 2012-09-10 |
Sponsor Name:Charité, Universitätsmedizin Berlin | ||
Full Title: Investigation of nociceptive and antinociceptive mechanisms under anesthesia using fMRI, EEG and noxious reflexes | ||
Medical condition: This is a CT including only healthy volunteers. The aim of the study is to investigate the effect of a commonly used anesthetic drug in clinical concentrations on nociceptive and antinociceptive me... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-005043-86 | Sponsor Protocol Number: 1308143 | Start Date*: 2014-03-21 | |||||||||||
Sponsor Name:CHU de Saint-Etienne | |||||||||||||
Full Title: Reactivity of the autonomic nervous system after a nociceptive stress in the newborn: Interest of sucrose and non-nutritive sucking. | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005701-20 | Sponsor Protocol Number: ANST2015_1 | Start Date*: 2015-05-20 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Shifting pain modulation towards anti-nociceptivity: Mechanism-specific pharmacological prevention of post sternotomy pain: the MASTER study | ||
Medical condition: chronic pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005086-20 | Sponsor Protocol Number: CHDR1117 | Start Date*: 2011-11-22 |
Sponsor Name:Centre for Human Drug Research (CHDR) | ||
Full Title: Effects of paracetamol on nociception in adolescents. | ||
Medical condition: Nociceptive pain (disorders) | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-010428-25 | Sponsor Protocol Number: KF5503/45 | Start Date*: 2010-02-15 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: An evaluation of the effectiveness and tolerability of tapentadol hydrochloride prolonged release, and tapentadol hydrochloride immediate release on demand, in subjects with severe chronic nocicept... | |||||||||||||
Medical condition: Low back Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) NL (Completed) DE (Completed) FR (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008721-29 | Sponsor Protocol Number: KYT62121/2008-01 | Start Date*: 2009-11-19 | |||||||||||
Sponsor Name:Merck Selbstmedikation GmbH | |||||||||||||
Full Title: Double-blind, randomised, multi-centre, placebo-controlled clinical trail to investigate the efficacy and safety of a combination of comfrey root extract plus methyl nicotinate versus a preparation... | |||||||||||||
Medical condition: Acute upper or low back pain as described in the note for guidance on clinical investigation of medical products for treatment of Nociceptive Pain (CPMP/EWP/612/00. Nov. 21, 2002) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000864-41 | Sponsor Protocol Number: CHUB-patch-lidocaine | Start Date*: 2016-06-02 |
Sponsor Name:Centre Hospitalier Universitaire Brugmann | ||
Full Title: A randomized controlled trial of lidocaine patch for lower limb amputation pain. | ||
Medical condition: Lower limb amputation pain: phantom limb pain and primary/secondary scar hyperalgesia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-019591-67 | Sponsor Protocol Number: 1008032 | Start Date*: 2010-06-01 | |||||||||||
Sponsor Name:CHU de SAINT-ETIENNE | |||||||||||||
Full Title: Pain assessment during general anesthesia : DOLANS Study | |||||||||||||
Medical condition: perioperative analgesia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001769-14 | Sponsor Protocol Number: LACO15 | Start Date*: 2017-02-13 |
Sponsor Name:Javier E. Morales Sarabia | ||
Full Title: Analgesic efficacy of intravenous lacosamide administered perioperatively for thoracic surgery with thoracotomy approach. | ||
Medical condition: Acute postoperative pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000170-30 | Sponsor Protocol Number: MULTIPAIN-2-3-2013 | Start Date*: 2013-04-19 | |||||||||||
Sponsor Name:Mech-Sense, Aalborg University Hospital | |||||||||||||
Full Title: Effects of oxycodon and venlafaxine on human pain processing. A randomized, double-blinded, placebo-controlled, cross-over study | |||||||||||||
Medical condition: Healthy volunteers - pain | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013022-16 | Sponsor Protocol Number: ZonMw 80-82100-98-096/11510014 | Start Date*: 2009-10-21 | |||||||||||
Sponsor Name:Erasmus MC [...] | |||||||||||||
Full Title: Effecten en bijwerkingen van opioïden: een studie naar de rol van farmacokinetische en farmacogenetische heterogeniteit. | |||||||||||||
Medical condition: Nociceptive cancer pain for which strong opioids are needed | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003621-87 | Sponsor Protocol Number: COIL | Start Date*: 2007-02-21 | |||||||||||
Sponsor Name:Merck Selbstmedikation GmbH | |||||||||||||
Full Title: Double-blind, placebo-controlled, randomised, parallel-groups, multi-centre clinical trial for the evaluation of efficacy and safety of an ointment of comfrey extract in comparison to placebo in th... | |||||||||||||
Medical condition: Acute upper and low back pain as described in the note for guidance on clinical investigation of medical products for treatment of Nociceptive Pain. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002557-56 | Sponsor Protocol Number: ACT11705 | Start Date*: 2011-11-24 | |||||||||||
Sponsor Name:sanofi-aventis | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, placebo-controlled study to assess the clinical benefit of SSR411298 as adjunctive treatment for persistent cancer pain | |||||||||||||
Medical condition: cancer pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010427-12 | Sponsor Protocol Number: KF5503/44 | Start Date*: 2009-10-14 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: An evaluation of the effectiveness and tolerability of tapentadol hydrochloride prolonged release, and tapentadol hydrochloride immediate release on demand, in subjects with uncontrolled severe chr... | |||||||||||||
Medical condition: Low back Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) AT (Completed) DE (Completed) IT (Completed) PL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002302-43 | Sponsor Protocol Number: CHDR1209 | Start Date*: 2012-06-08 | ||||||||||||||||
Sponsor Name:Dr. Reddy's Laboratories Ltd. | ||||||||||||||||||
Full Title: A study to investigate the analgesic effects of buprenorphine and milnacipram in healthy volunteers. | ||||||||||||||||||
Medical condition: Pain therapeutics, neuropathic pain, nociceptive pain, synergism between opioids and TCA. | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-006184-70 | Sponsor Protocol Number: PM07/8404 | Start Date*: 2009-01-09 |
Sponsor Name:The Leeds Teaching Hospitals NHS Trust | ||
Full Title: A POPULATION STUDY INTO THE PREVALENCE AND GENETIC PROFILE OF PATIENTS WITH CHRONIC PAIN WHO DO NOT RESPOND TO ORAL CODEINE A single site, pilot population study into the prevalence and genetic p... | ||
Medical condition: Chronic pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000141-52 | Sponsor Protocol Number: Landscaping_2017 | Start Date*: 2017-04-03 | |||||||||||
Sponsor Name:Asbjørn Mohr Drewes | |||||||||||||
Full Title: The effect of tapentadol on the human pain system: A study based on advanced neurophysiology and imaging techniques to illustrate the mechanism of tapentadol and oxycodone in the central, autonomic... | |||||||||||||
Medical condition: Healthy volunteers - pain | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016457-18 | Sponsor Protocol Number: E05-CL-3001 | Start Date*: 2010-07-20 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd | |||||||||||||
Full Title: A Multicentre, Single-Arm, Open-Label Study Of The Repeated Administration Of QUTENZA For The Treatment Of Peripheral Neuropathic Pain | |||||||||||||
Medical condition: Peripheral Neuropathic Pain in Postherpetic Neuralgia (PHN), Painful HIV-Associated Neuropathy (HIV-AN), Peripheral Neuropathic Injury (PNI), Idiopathic Small Nerve Neuropathy (ISNN) or other Perip... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) FR (Completed) BE (Completed) GB (Completed) CZ (Completed) FI (Completed) ES (Completed) AT (Completed) IT (Completed) HU (Completed) NL (Completed) SK (Completed) PL (Completed) SI (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001523-24 | Sponsor Protocol Number: 14744001 | Start Date*: 2016-03-25 | |||||||||||
Sponsor Name:UHToulouse | |||||||||||||
Full Title: Evaluation of the analgesic effects of prolonged-release oxycodone and of L-Dopa, versus placebo, on central neuropathic pain in Parkinson's disease : OXYDOPA trial | |||||||||||||
Medical condition: Central neuropathic pain in Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004097-15 | Sponsor Protocol Number: GabA-01 | Start Date*: 2015-10-23 |
Sponsor Name:Wilhelminenspital | ||
Full Title: A single center, prospective, randomized, double blind, placebo-controlled, three-way cross-over study of the analgesic effects of Midazolam versus Placebo with Fentanyl as an active control in hum... | ||
Medical condition: nociceptive pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
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